Familial Genetic Generalised Epilepsies

Gene: PRRT2

Red List (low evidence)

PRRT2 (proline rich transmembrane protein 2)
EnsemblGeneIds (GRCh38): ENSG00000167371
EnsemblGeneIds (GRCh37): ENSG00000167371
OMIM: 614386, Gene2Phenotype
PRRT2 is in 15 panels

1 review

Richard Scott (Genomics England Curator)

Comment on list classification: Insufficient data for this phenotype
Created: 8 May 2016, 7 p.m.

History Filter Activity

8 May 2016, Gel status: 1

Gene classified by Genomics England curator

Richard Scott (Genomics England Curator)

This gene has been classified as Red List (Low Evidence).

6 May 2015, Gel status: 2

Added New Source

Eik Haraldsdottir (Genomics England)

PRRT2 was added to Familial generalised epilepsypanel. Sources: Radboud University Medical Center, Nijmegen

6 May 2015, Gel status: 1

Added New Source

Eik Haraldsdottir (Genomics England)

PRRT2 was added to Familial generalised epilepsypanel. Sources: UKGTN